檢索結果 - Mohammed Genead

Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration 由 Robert K. Koenekoop, Hui Wang, Jacek Majewski, Xia Wang, Irma López, Huanan Ren, Yiyun Chen, Yumei Li, Gerald A. Fishman, Mohammed Genead, Jeremy Schwartzentruber, Naimesh Solanki, Elias I. Traboulsi, Jingliang Cheng, Clare V. Logan, Martin McKibbin, Bruce E. Hayward, David Parry, Colin A. Johnson, Mohammed Nageeb, James A. Poulter, Moin Mohamed, Hussain Jafri, Yasmin Abdul Rashid, Graham R. Taylor, Vafa Keser, Graeme Mardon, Huidan Xu, Chris F. Inglehearn, Qing Fu, Carmel Toomes, Rui Chen

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